The following data is part of a premarket notification filed by Mectron Spa with the FDA for Piezosurgery White.
| Device ID | K151248 |
| 510k Number | K151248 |
| Device Name: | PIEZOSURGERY WHITE |
| Classification | Drill, Bone, Powered |
| Applicant | MECTRON SPA VIA LORETO 15 Carasco, IT 16042 |
| Contact | Mr. Franco Zunino |
| Correspondent | Mr. Roger Gray Donawa Lifescience Consulting S.r.l. Piazza Albania, 10 Rome, IT 00153 |
| Product Code | DZI |
| CFR Regulation Number | 872.4120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-05-11 |
| Decision Date | 2015-09-04 |